One millisecond fixation time might be an excessive requirement, but in order to perform an emulation accurate enough to preserve the self, you will probably need much more detail than the network topology and some statistics. Synapses have fine surface features that may well be relevant, and neurons may have relevant internal state stored as DNA methylation patterns, concentrations of various chemical, maybe even protein folding states. Some of these features are probably difficult to preserve and possibly difficult to scan.
The surface details we can read with SEM, and we can observe chemical/protein concentrations through immunostaining and sub-wavelength optical microscopy (SEM and SWOM hybrid is my bet for the technology we wind up using). I don't think there's strong evidence for DNA methylation or protein state being used for long-term data storage. If evidence arises, we'll re-evaluate then. But modern neuron models don't account for those, and, again, function realistically, so they're not critical for the computation. The details we're reading likely wouldn't have to be simulated outright - they would just alter the shape of the probability distribution your simulation is sampling from. A lot of the fine stuff is so noisy, it isn't practical to store data in it. The stuff we know is involved we can definitely preserve. As a general rule, if the data is lost within minutes of death, it's probably also lost during the average workday.
Actually they vitrified 475 micrometre slices of the hippocampus of rat brains. It's no mystery that small samples can be vitrified without using toxic concentrations of cryoprotectants.
I honestly don't think cryoprotectant damage is anywhere near the big problem here. I'm sure it does cellular damage, but it seems to leave cell morphology essentially intact, and isn't reactive enough to really screw up most of the things we know we have to care about, in terms of cell state. Ischemia is a bigger problem, and one of my points of skepticism about non-standby cryonics. Four plus hours at room temperature simply seems too long. That said, as our understanding of cell death improves, we're starting to notice that most brain death seems to be failure of the cells' oxygen metabolisms, not failure of synaptic linkings. I'd like to see studies done on exactly how long it takes relevant neural details to begin to break down at room temperature. That said, flatlining cases suggest that there's some reason to hope for the time being. I'd like to see the science done, in any case.
If you don't believe in an afterlife, then it seems you currently have two choices: cryonics or permanent death. Now, I don't believe that cryonics is pseudoscience, but it's still pretty poor odds (Robin Hanson uses an estimate of 5% here). Unfortunately, the alternative offers a chance of zero. I see five main concerns with current cryonic technology:
So I wonder if we can do better.
I recall reading of juvenile forms of amphibians in desert environments that could survive for decades of drought in a dormant form, reviving when water returned. One specimen had sat on a shelf in a research office for over a century (in Arizona, if I recall correctly) and was successfully revived. Note: no particular efforts were made to maintain this specimen: the dry local climate was sufficient. It was suggested at the time that this could make an alternative method of preserving organs. Now the advantages of this approach (which I refer to flippantly as "dryonics") is:
There is one big disadvantage of this approach, of course: no one knows how to do it (it's not entirely clear how the juvenile amphibians do it) or even if it would be possible in larger, more complex organisms. And, so far as I know, no one is working on it. But it would seem to offer a much better prospect than our current options, so I would suggest it worth investigating.
I am not a biologist, and I'm not sure where one would start developing such a technology. I frankly admit that I am sharing this in the hope that someone who does have an idea will run with it. If anyone knows of any work on these lines, or has an idea how to proceed, please send a comment or email. Or even if you have another alternative. Because right now, I don't consider our prospects good.
[Note: I am going on memory in this post; I really wish I could provide references, but there does not seem much activity along these lines that I can find. I'm not even sure what to call it: mummification? Probably too scary. Dehydration? Anyway feel free to add suggestions or link references.]